FDA 510(k) Applications Submitted by David H Mueller

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971756	05/12/1997	MEDTRONIC MODEL 3998 LEAD	MEDTRONIC VASCULAR
K011584	05/23/2001	MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF	MEDTRONIC VASCULAR
K972043	06/02/1997	MEDTRONIC MODEL 3273/3274 RF RECEIVER AND MODEL 3629/3630 SCREENER	MEDTRONIC VASCULAR
K972906	08/06/1997	MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)	MEDTRONIC VASCULAR
K953742	08/08/1995	BIFURCATED Y-EXTENSION	MEDTRONIC VASCULAR
K982902	08/14/1998	PERIPHERAL NERVE STIMULATION	MEDTRONIC VASCULAR
K222983	09/28/2022	NeuroBlate Fusion-S Software V3.17	Monteris Medical,
K964172	10/18/1996	MEDTRONIC MODEL 3991A, 3992A, 3993A, 3994A LEADS OR TRANSVERSE TRIPOLAR LEADS OR TTL	MEDTRONIC VASCULAR
K170724	03/09/2017	NeuroBlate System	Monteris Medical
K201056	04/21/2020	NeuroBlate System	Monteris Medical, Inc.
K171255	04/28/2017	Monteris Medical NeuroBlate System	Monteris Medical, Inc.
K182036	07/30/2018	NeuroBlate System	Monteris Medical
K172881	09/21/2017	NeuroBlate System	Monteris Medical
K162762	09/30/2016	NeuroBlate System	Monteris Medical, Inc.
K173305	10/18/2017	NeuroBlate System	Monteris Medical,
K193375	12/05/2019	NeuroBlate System	Monteris Medical
K041884	07/12/2004	MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS	MUELLER WATER CONDITIONING, INC.